USPatentGranted
B2

Imidazopyridyl compounds as aldosterone synthase inhibitors

Granted 3 Nov 2015 · 2 office actions

Current assignee: Merck Sharp & Dohme · originally Merck & Co., Inc.

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Inventors: D. Jonathan Bennett, Michael Lo, Jaiqiang Cai, Yusheng Xiong +10 · Examiner: Timothy R Rozof · AU 1625 · TC 1600

Life of the patent

4 dated events
⤢ drag to zoomJul 2011Jan 2012Jul 2012Jan 2013Jul 2013Jan 2014Jul 2014Jan 2015Jul 2015Jan 2016Prosecution
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Abstract

This invention relates to imidazopyridyl compounds of the structural formula: I or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as potentially to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthase. [structure]

Claims

9 · 1 independent · depth 2
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9 granted claims

Classifications

3 codes
IPC · International Patent Classification
Section A — Human necessities
  • A61K31/437
Section C — Chemistry; metallurgy
  • C07D487/04
  • C07D471/04

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File wrapper

Pendency
3.1 y
1,142 days filing → grant
Office actions
1
after a restriction
Responses
1
no RCE
Interviews
1
examiner interview summaries
Examiner
Timothy R Rozof
art unit 1625 · TC 1600
Citations: 58 back · 0 forward

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Chain of title

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Priority chain

2 priority documents
Priority
22 Sep 2011
earliest claimed
›Priority documents — 2
TypeDocumentDate
provisionalUS 6153791022 Sep 2011
related publicationUS 20140235667 A121 Aug 2014

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Citations

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